Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate

Base Information

• Chemical Name: Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate
• CAS No.: 912635-60-0
• Molecular Formula: C₁₅H₁₇N₃O₂
• Molecular Weight: 271.319
• Hs Code.: 2933990090
• Mol file: 912635-60-0.mol

Synonyms:ethyl 5-benzyl-4,6-dihydro-1H-pyrrolo[3,4-c]pyrazole-3-carboxylate;Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate;5-Benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylic acid ethyl ester

Chemical Property of Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate

Chemical Property:

• PSA: 58.22000
• LogP: 2.04010
• Storage Temp.: 2-8°C

Purity/Quality:

99% ^*data from raw suppliers

Ethyl5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate

There total 2 articles about Ethyl 5-benzyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-benzyl-3-pyrrolidinone (775-16-6) → C15H17N3O2 (912635-60-0)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol

2: H₂NNH₂

With hydrazine; In ethanol;

DOI:10.1016/j.bmcl.2007.06.028

Reference yield:

C15H19N3O3 → C15H17N3O2 (912635-60-0)

Guidance literature:

With acetic acid; at 70 ℃; for 3h;

DOI:10.1071/CH13468

Reference yield:

C15H17N3O2 (912635-60-0) → C6H7N3O2

Guidance literature:

Multi-step reaction with 2 steps

1: Alkaline hydrolysis

DOI:10.1016/j.bmcl.2007.06.028

upstream raw materials:

N-benzyl-3-pyrrolidinone

Downstream raw materials:

C₁₃H₁₃N₃O₂

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